SUCCESSFUL T-CELL PRIMING IN B-CELL-DEFICIENT MICE

被引:269
作者
EPSTEIN, MM [1 ]
DIROSA, F [1 ]
JANKOVIC, D [1 ]
SHER, A [1 ]
MATZINGER, P [1 ]
机构
[1] NIAID, PARASIT DIS LAB, BETHESDA, MD 20892 USA
关键词
D O I
10.1084/jem.182.4.915
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B cells are an abundant population of lymphocytes that can efficiently capture, process, and present antigen for recognition by activated or memory T cells. Controversial experiments and arguments exist, however, as to whether B cells are or should be involved in the priming of virgin T cells in vivo. Using B cell-deficient mice, we have studied the role of B cells as antigen-presenting cells in a wide variety of tests, including assays of T cell proliferation and cytokine production in responses to protein antigens, T cell killing to minor and major histocompatibility antigens, skin graft rejection, and the in vitro and in vivo responses to shistosome eggs. We found that B cells are not critical for either CD4 or CD8 T cell, priming in any of these systems. This finding lends support to the notion that the priming of T cells is reserved for specialized cells such as dendritic cells and that antigen presentation by B cells serves distinct immunological functions.
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页码:915 / 922
页数:8
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